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- ...and project management teams to ensure trials comply with Good Clinical Practice (GCP) and regulatory requirements. Work with pharmacovigilance teams to ensure timely and accurate safety reporting and management of safety signals during the trial. Represent Medical...SuggestedFull timeWork at officeWorldwide
- ...SOPs, ICH GCP and country regulations. This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA). Supports Inspection Readiness for clinical trial management scope. Oversees CRAs and Central...SuggestedContract workImmediate start
- ...Continuously ensure compliance with global and local procedures, national and international regulations, standards and guidelines for all pharmacovigilance of our products; Support ongoing projects within the PSP Innovations Team. Fulfil other duties as required....SuggestedFull timeWork at officeLocal areaRemote workFlexible hoursAfternoon shift
- ...subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review...SuggestedContract workInterim roleLocal areaImmediate startRemote work
- ...(s) assigned to the trial Reviews protocol deviations Reviews RAE reports, writes and/or reviews SAE narratives, supports Pharmacovigilance team with outstanding safety queries, interacts with sponsor on site safety issues Reviews IND/SUSAR Safety Reports, updates/...SuggestedFull timeContract workWork from home
- ...Works in partnership internally with Global Clinical Trial Organization (GCTO) country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, Headquarter (HQ) functional areas and externally with vendors and sites, Internal Review...SuggestedRemote jobContract workWork at officeLocal area
- ...About the Role: We are seeking Patient Safety Specialists to join our team, working closely with our global pharmacovigilance teams across clinical trials and post-marketed projects. The successful candidate will contribute to the execution of safety processes with increasing...SuggestedFreelanceLocal area
- ...into Traditional Chinese (Hong Kong) for below material: LS-Non-Clinical-Technical LS-Healthcare Marketing Medical LS-Pharmacovigilance LS-CMC LS-Clinical-Legal Qualifications, Skills & Experience: Excellent written and verbal communication skills in...SuggestedHourly payLong term contractFreelanceRemote work
- ...Ensure timely and compliant reporting of Adverse Events (AEs) and Product Quality Complaints (PQCs) in accordance with Health Canada pharmacovigilance requirements and guidelines, including accurate documentation, appropriate escalation, and effective collaboration with internal...SuggestedPermanent employmentFull timeWork at officeRemote work
Bayshore HealthCare
Remote19 days ago
